苯巴比妥在中国人群中的生物等效性:考虑食物对药代动力学的作用。

IF 1.8 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Wang Xinman, Liu Yuan, Sun Ying, Wang Yiyun
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引用次数: 0

摘要

癫痫是世界上最严重的神经系统疾病之一,可能严重危及患者的生命。苯巴比妥是临床上治疗癫痫的重要药物,在全身性强直阵挛性发作、局灶性发作、癫痫持续状态、小儿癫痫的治疗中具有不可替代的作用。然而,苯巴比妥的原研药尚未在中国上市。因此,一种经济有效的仿制药对患者来说意义重大。本研究采用单中心、随机、开放标签、单剂量、双制剂、两期、双序列交叉设计和平行设计。以山东新华制药有限公司生产的苯巴比妥片为试验配方,以富士永制药有限公司生产的苯巴比妥片为参比配方进行生物等效性研究。此外,还研究了食物对其药代动力学参数的影响。结果表明,试验制剂与对照制剂具有生物等效性,食品可降低苯巴比妥的最大浓度和暴露量。本研究为苯巴比妥仿制药的上市提供数据支持,为苯巴比妥的合理用药提供理论依据。临床试验已在中国临床试验注册中心注册(注册号:CTR20242404和CTR20244155)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phenobarbital Bioequivalence in Chinese Population: Considering the Role of Food on Pharmacokinetics.

Epilepsy is one of the most severe neurological disorders in the world, which might seriously endanger the lives of patients. Phenobarbital is an important medicine clinically used for the treatment of epilepsy, and it is irreplaceable in the treatment of generalized tonic-clonic seizures, focal seizures, status epilepticus, and pediatric epilepsy. However, the original research medicine of phenobarbital has not been launched in China. Therefore, an economical and effective generic medicine is of great significance to patients. In this study, a single-center, randomized, open-label, single-dose, two-formulation, two-period, two-sequence crossover design and parallel design were adopted. The phenobarbital tablets produced by Shandong Xinhua Pharmaceutical Co., Ltd. were used as the test formulation, and Phenobal produced by Fujinaga Pharmaceutical Co., Ltd. was used as the reference formulation for a bioequivalence study. Additionally, the influence of food on the pharmacokinetic parameters al was investigated. The results showed that the test formulation and the reference formulation were bioequivalent, and food might reduce the Cmax (maximum concentration) and exposure of phenobarbital. This study provides data support for the marketing of generic phenobarbital medicines and offers a theoretical basis for the rational administration of phenobarbital. The clinical trial was registered in Chinese Clinical Trial Registry (Registration numbers: CTR20242404 and CTR20244155).

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来源期刊
CiteScore
3.70
自引率
10.00%
发文量
154
期刊介绍: Clinical Pharmacology in Drug Development is an international, peer-reviewed, online publication focused on publishing high-quality clinical pharmacology studies in drug development which are primarily (but not exclusively) performed in early development phases in healthy subjects.
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